Concepedia

Reduction of β-ketosulfoxides : a highly efficient asymmetric synthesis of both enantiomers of methyl carbinols from the corresponding esters

Guy Solladié, Christine Greck, Gilles Demailly, Arlette Solladié‐Cavallo

Tetrahedron Letters · 1982 · 83 citations · 11 references

DOI

Concepts

References

11

Asymmetric Synthesis Using Nucleophilic Reagents Containing a Chiral Sulfoxide Group

Guy Solladié · Synthesis · 1981 · 371 citations

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Chelation-controlled nucleophilic additions. 1. A highly effective system for asymmetric induction in the reaction of organometallics with α-alkoxyketones.

W. Clark Still, John H. McDonald · Tetrahedron Letters · 1980 · 310 citations

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Chelation-controlled nucleophilic additions. 2. A highly effective system for asymmetric induction in the reaction of organometallics with β-alkoxyaldehydes.

W. Clark Still, Josef A. Schneider · Tetrahedron Letters · 1980 · 176 citations

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CCVII.—Investigations on the dependence of rotatory power on chemical constitution. Part IV. The rotations of the normal secondary alcohols of the formula C<sub>2</sub>H<sub>5</sub>·CH(OH)·R

Robert Howson Pickard, Joseph Kenyon · Journal of the Chemical Society Transactions · 1913 · 57 citations · Full text

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Asymmetric synthesis using α-sulfinylcarbanions. I. Synthesis of optically active alcohols

Gen-ichi Tsuchihashi, Shinobu Iriuchijima, Mariko Ishibashi · Tetrahedron Letters · 1972 · 47 citations

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